Beschreibung
Drug Regulatory Affairs Manager (m/f/d)
Reference: -en
Start: 12/19
Duration: 7 MM
Main tasks:
- Preparation of the regulatory strategy for new submissions
- Timely submission of new products to Swissmedic in agreement with the yearly target
- Strategic business partner to Business Development, Quality Assurance, Supply Chain as well as for other Global Regulatory Groups (RCCs)
- Drive product maintenance to ensure regulatory compliance
- Obtain a number of marketing authorizations in accordance with the yearly target
Main qualifications
- Education: Pharmacist or natural scientist preferably with medical background
- Languages: German (fluent), English (intermediate to advanced) and French (desirable)
- Experience: Intermediate
- Experience and know-how in Drug Regulatory Affairs and project management. Knowledge of Swiss regulations and guidelines
Main advantages:
- Support with job starts, career changes and re-entries
- We will create a candidate profile containing your strengths and potential and thus increase your chance of being placed in a position
- We will give you valuable tips and feedback on your application documents and interviews
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
My contact person:
Mihai-Lucian Burcea
Referencenumber:
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